论文著作:
45. Hu, Q.-Q.#; Geng, Z.-X.#; Bai, X.; Chen, J.*; Zhou, L.* Lewis Acid Catalyzed Divergent Reaction of Bicyclo[1.1.0]butanes with Quinones for the Synthesis of Diverse Polycyclic Molecules. Angew. Chem. Int. Ed. 2025, 64, e202506228.
44. Hu, Q.-Q.#; Wang, L.-Y.#; Chen, X.-H.; Geng, Z.-X.; Chen, J.*; Zhou, L.* Lewis Acid Catalyzed Cycloaddition of Bicyclobutanes with Ynamides for the Synthesis of Polysubstituted 2-Amino-bicyclo[2.1.1]hexenes. Angew. Chem. Int. Ed. 2024, 63, e202405781.
43. Xu, W.-L.#; Zhang, R.-X.#; Wang, H.; Chen, J. *; Zhou, L.* Helicoselective Synthesis of Indolohelicenoids through Organocatalytic Central-to-Helical Chirality Conversion. Angew. Chem. Int. Ed. 2024, 63, e202318021.
42. Wang, C.-J.#; Meng, H.-J.#; Tang, Y.; Chen, J.*; Zhou, L.* Aromatic Amine and Chiral Phosphoric Acid Synergistic Catalyzed Cascade Reaction of Alkynylnaphthols with Aldehydes. Org. Lett. 2024, 26, 1489-1494.
41. Sun, H.-R.#; Yang, L.#; Li, Y.; Yu, L.; Gou, B.-B.; Sharif, A.; Jian, Q.-S.; Chen, J.*; Zhou, L.* Organocatalytic Asymmetric [2+2] Cycloaddition of Alkynes with Quinones. Sci. China Chem. 2023, 66, 2292-2299.
40. Sun, H.-R.#; Sharif, A.#; Chen, J.*; Zhou, L.*, Atroposelective Synthesis of Heterobiaryls through Ring Formation. Chem. Eur. J. 2023, 29, e202300183。
39. Gou, B.-B.#; Tang, Y.#; Lin, Y.-H.#; Yu, L.; Jian, Q.-S.; Sun, H.-R.; Chen, J.; Zhou, L.*, Modular Construction of Heterobiaryl Atropisomers and Axially Chiral Styrenes via All-Carbon Tetrasubstituted VQMs. Angew. Chem. Int. Ed. 2022, 61, e202208174.
38. Yang, H.#; Sun, H.-R.#; He, R.-Q.; Yu, L.; Hu, W.; Chen, J.; Yang, S.; Zhang, G.-G.; Zhou, L.*, Organocatalytic cycloaddition of alkynylindoles with azonaphthalenes for atroposelective construction of indole-based biaryls. Nat. Commun. 2022, 13, 632.
37. Sharif, A.#; Sun, H.-R.#; Xu, W.-L.; Gou, B.-B.; Yang, L.; Li, Y.; Chen, J.*; Zhou, L.*, A Dehydrogenative Inverse Electron Demand Diels–Alder Reaction for the Synthesis of Functionalized Pyranones. Org. Lett. 2022, 24, 4316-4321.
36. Xu, W.-L.#; Zhao, W.-M.#; Zhang, R.-X.; Chen, J.; Zhou, L.*, Organocatalytic cycloaddition–elimination cascade for atroposelective construction of heterobiaryls. Chem. Sci. 2021, 12, 14920-14926.
35. Yang, H.#; Xu, W.-L.#; Zeng, X.-Y.; Chen, J.; Yu, L.*; Zhou, L.*, Hydrogen Bond Assisted Central-to-Spiro Chirality Transfer and Central-to-Axial Chirality Conversion: Asymmetric Synthesis of Spirocycles. Org. Lett. 2021, 23, 9315-9320.
34. Yang, H.; Chen, J.; Zhou, L.*, Construction of Axially Chiral Compounds via Central-to-Axial Chirality Conversion. Chemistry – An Asian Journal 2020, 15, 2939-2951.(Invited review)
33. Xu, W.-L.#; Hu, W.#; Zhao, W.-M.; Wang, M.; Chen, J.*; Zhou, L.*, Copper(I)/DDQ-Mediated Double-Dehydrogenative Diels–Alder Reaction of Aryl Butenes with 1,4-Diketones and Indolones. Org. Lett. 2020, 22, 7169-7174.
32. Wang, S.-J.#; Wang, Z.#; Tang, Y.; Chen, J.*; Zhou, L.*, Asymmetric Synthesis of Quinoline-Naphthalene Atropisomers by Central-to-Axial Chirality Conversion. Org. Lett. 2020, 22, 8894-8898.
31. Sun, H.-R.#; Zhao, Q.#; Yang, H.; Yang, S.; Gou, B.-B.; Chen, J.; Zhou, L.*, Chiral Phosphoric-Acid-Catalyzed Cascade Prins Cyclization. Org. Lett. 2019, 21, 7143-7148.
30. Gou, B.-B.; Liu, H.-F.; Chen, J.*; Zhou, L.*, Palladium-Catalyzed Site-Selective C(sp3)–H Arylation of Phenylacetaldehydes. Org. Lett. 2019, 21, 7084-7088.
29. Hu, Y.-L.#; Wang, Z.#; Yang, H.#; Chen, J.; Wu, Z.-B.; Lei, Y.; Zhou, L.* Conversion of two stereocenters to one or two chiral axes: atroposelective synthesis of 2,3-diarylbenzoindoles. Chem. Sci. 2019, 10, 6777-6784. (Back cover)
28. Xu, W.-L.; Tang, L.; Ge, C.-Y.; Chen, J.*; Zhou, L.* “Synthesis of Tetrahydroisoindolinones via a Metal-Free Dehydrogenative Diels-Alder Reaction” Adv. Synth. Catal. 2019, 361, 2268-2273.
27. Gou, B.-B.; Yang, H.; Sun, H.-R.; Chen, J.*; Wu, J.*; Zhou, L.* “Phenanthrene Synthesis by Palladium(II)-Catalyzed γ-C(sp2)–H Arylation, Cyclization, and Migration Tandem Reaction” Org. Lett. 2019, 21, 80-84.
26. Xu, W.-L.; Zhang, H.; Hu, Y.-L.; Yang, H.; Chen, J.*; Zhou, L.* “Metal-Free Dehydrogenative Diels–Alder Reactions of Prenyl Derivatives with Dienophiles via a Thermal Reversible Process”Org. Lett. 2018, 20, 5774-5778.
25. Feng, W.#; Yang, H.#; Wang, Z.; Gou, B.-B.; Chen, J.*; Zhou, L.* “Enantioselective [3 + 2] Formal Cycloaddition of 1-Styrylnaphthols with Quinones Catalyzed by a Chiral Phosphoric Acid” Org. Lett. 2018, 20, 2929-2933.
24. Zhao, M.#; Liu, J.-L.#; Liu, H.-F.; Chen, J.*; Zhou, L.* “Construction of Bisbenzopyrone via N-Heterocyclic Carbene Catalyzed Intramolecular Hydroacylation–Stetter Reaction Cascade” Org. Lett. 2018, 20, 2676-2679.
23. Wang, J.-J.#; Yang, H.#; Gou, B.-B.; Zhou, L.*; Chen, J.* “Enantioselective Organocatalytic Sulfenylation of β-Naphthols” J. Org. Chem. 2018, 83, 4730-4738.
22. Zhao, M.#; Zhang, Y.-T.#; Chen, J.*; Zhou, L.* “Enantioselective Reactions Catalyzed by N-Heterocyclic Carbenes” Asian J. Org. Chem. 2018, 7, 54-69.(Invited review)
21. Liu, J.-L.; Zhang, Y.-T.; Liu, H.-F.; Zhou, L.*; Chen, J.* “N-Heterocyclic Carbene Catalyzed Stereoselective Glycosylation of 2-Nitrogalactals” Org. Lett. 2017, 19, 5272-5275.
20. Li, X.-Q.#; Yang, H.#; Wang, J.-J.; Gou, B.-B.; Chen, J.*; Zhou, L.* "Asymmetric Arylative Dearomatization of β-Naphthols Catalyzed by a Chiral Phosphoric Acid" Chem. Eur. J. 2017, 23, 5381-5385.
19. Yang, H.; Fan, G.-T.; Zhou, L.*; Chen, J.* “Enantioselective Chloro-O-cyclization of Unsaturated N-Tosylcarbamates”. Adv. Synth. Catal. 2017, 2017, 359, 1295-1300..
18. Zhao, M.; Chen, J.*; Yang, H.; Zhou, L.* “N-Heterocyclic Carbene-Catalyzed Intramolecular Nucleophilic Substitution: Enantioselective Construction of All-Carbon Quaternary Stereocenters”. Chem. Eur. J. 2017, 23, 2783-2787.
17. Dong, Y.-T.; Jin, Q.; Zhou, L.*; Chen, J.* “N-Heterocyclic Carbene Catalyzed Sulfenylation of α,β-Unsaturated Aldehydes”. Org. Lett. 2016, 18, 5708-5711.
16. Wang, Y.-Y.; Sun, M.-H.; Zeng, N.-N.; Chen, J.*; Zhou, L.* “Metal-Free Amidation of Ethers with N,N-Dibromosulfonamides”. Synlett 2016, 27, 1438-1442.
15. Feng, H.-X.; Wang, Y.-Y.; Chen, J.*; Zhou, L.* “A Dehydrogenative Diels–Alder Reaction of Prenyl Derivatives with 2,3-Dichloro-5,6-dicyanobenzoquinone”. Adv. Synth. Catal. 2015, 357, 940-944.
14. Qi, J.#; Fan, G.-T.#; Chen, J.; Sun, M.-H.; Dong, Y.-T.; Zhou, L.* “Catalytic enantioselective bromoamination of allylic alcohols” Chem. Commun. 2014, 50, 13841-13844.
13. Zhao, M.; Yang, H.; Li, M.-M.; Chen, J.*; Zhou, L.* “N-Heterocyclic Carbene Catalyzed Intramolecular Acylation of Allylic Electrophiles” Org. Lett. 2014, 16, 2904-2907.
12. Fan, G.-T.; Sun, M.-H.; Gao, G.; Chen, J.*; Zhou, L.* “Regioselective Bromocyclization of Unsaturated N-Tosylcarbamates Promoted by N,N-Dibromosulfonamides” Synlett 2014, 25, 1921-1925.
11. Chen, J.; Guo, Y.-P.; Sun, M.-H.; Fan, G.-T.; Zhou, L.* “Bromoform reaction of tertiary amines with N,N-dibromosulfonamides or NBS/sulfonamides” Chem. Commun. 2014, 50, 12367-12370.
10. Chen, J.; Zhou, L.* “Recent Progress in the Asymmetric Intermolecular Halogenation of Alkenes” Synthesis 2014, 46, 586-595. (Invited review)
9. Zhou, L.; Tay, D. W.; Chen, J. Leung, G. Y. C.; Yeung, Y.-Y. “Enantioselective synthesis of 2-substituted and 3-substituted piperidines through a bromoaminocyclization process”. Chem. Commun. 2013, 49, 4412-4414.
8. Zhou, L.; Chen, J.; Tan, C. K.; Yeung, Y.-Y. “Enantioselective Bromoaminocyclization Using Amino-Thiocarbamate Catalyst”, J. Am. Chem. Soc. 2011, 133, 9164-9167. (Featured as a cover article, and highlighted in Synfacts 2011, 787)
7. Zhou, L.; Zhou, J.; Tan, C. K.; Chen, J.; Yeung, Y.-Y. “N-Bromosuccinimide Initiated One-pot Synthesis of Imidazoline”, Org. Lett. 2011, 13, 2448-2451.
6. Zhou, L.; Chen, J.; Zhou, J.; Yeung, Y.-Y. “N-Bromosuccinimide Promoted One-Pot Synthesis of Guanidine: Scope and Mechanism”, Org. Lett. 2011, 13, 5804-5807.
5. Zhou, L.; Tan, C. K.; Jiang, X.; Chen, F.; Yeung, Y.-Y. “Asymmetric Bromolactonization Using Amino-thiocarbamate Catalyst”, J. Am. Chem. Soc. 2010, 132, 15474-15476. (Top 10 most-accessed article from the JACS in Oct 2010, and highlighted in Synfacts 2011, 92)
4. Zhou, L.; Tan, C. K.; Zhou, J.; Yeung, Y.-Y. “Facile, Efficient, and Catalyst-Free Electrophilic Aminoalkoxylation of Olefins: Scope and Application”, J. Am. Chem. Soc. 2010, 132, 10245-10247.
3. Zhou, L.; Zhang, T.-X.; Li, B.-R.; Cao, X.-P. Kuck, D. “C3v-Symmetrical Tribenzotriquinacenes Extended by Six C1-Functional Groups and the First Triquinacene-based Tris(dithiametacyclophanes)”, J. Org. Chem. 2007, 72, 6382-6389.
2. Zhou, L.; Chen, J.; Cao, X.-P. “An Efficient Synthesis of Functionalized Pyrrolidines and 5-epi-Hyacinthacine A4 from D-Glucose”, Synthesis 2007, 1359-1365.
1. Zhou, L.; Cao, X.-P.; Neumann, B.; Stammler, H.-G.; Kuck, D. “Multiple Stille Cross-Coupling Reactions with Tribenzotriquinacenes and Fenestrindanes”. Synlett 2005, 2771-2775.